Product Details
- SNP ID
-
rs150204038
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.20:31665964 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CAGTGTCTGGTCATTTCCGACTGAA[C/G]AGTGAGCCCAGCAGAACCACGCCGG
- Phenotype
-
MIM: 600039
- Polymorphism
- C/G, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
BCL2L1
PubMed Links
Gene Details
- Gene
- BCL2L1
- Gene Name
- BCL2 like 1
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001191.3 |
1064 |
Silent Mutation |
CTC,CTG |
L166L |
NP_001182.1 |
| NM_001317919.1 |
1064 |
Silent Mutation |
CTC,CTG |
L229L |
NP_001304848.1 |
| NM_001317920.1 |
1064 |
Silent Mutation |
CTC,CTG |
L229L |
NP_001304849.1 |
| NM_001317921.1 |
1064 |
Silent Mutation |
CTC,CTG |
L229L |
NP_001304850.1 |
| NM_001322239.1 |
1064 |
Silent Mutation |
CTC,CTG |
L229L |
NP_001309168.1 |
| NM_001322240.1 |
1064 |
Silent Mutation |
CTC,CTG |
L229L |
NP_001309169.1 |
| NM_001322242.1 |
1064 |
Silent Mutation |
CTC,CTG |
L229L |
NP_001309171.1 |
| NM_138578.2 |
1064 |
Silent Mutation |
CTC,CTG |
L229L |
NP_612815.1 |
| XM_011528964.2 |
1064 |
Silent Mutation |
CTC,CTG |
L229L |
XP_011527266.1 |
| XM_017027993.1 |
1064 |
Silent Mutation |
CTC,CTG |
L229L |
XP_016883482.1 |
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